MAUDE Adverse Event Report: FISHER & PAYKEL HEALTHCARE LTD OPTIFLOW + TRACHEOSTOMY INTERFACE; BTT

Model Number	OPT970E
Medical Device Problem Code	Material Split, Cut or Torn (4008)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).We are currently in the process of completing our investigation.We will provide a follow up report upon completion of the investigation.
Event or Problem Description
A distributor in canada reported that the tubing of an opt970 optiflow + tracheostomy direct connection was found damaged during patient use.There were no patient consequences.
Event or Problem Description
A distributor in canada reported that the tubing of an opt970e optiflow + tracheostomy direct connection was found damaged during patient use.There were no patient consequences.
Additional Manufacturer Narrative
(b)(4).The opt970e optiflow + tracheostomy direct connection interface is used to deliver humidified oxygen to patients via tracheostomy.The interface is held in place by a neck strap and also includes a lanyard which is placed around the patient's neck or attached to the patient's clothing or bedding to remove the load of the breathing circuit from the patient's trache.Method: the complaint opt970e optiflow + tracheostomy direct connection interface was returned to fisher & paykel healthcare (f&p) where it was visually inspected.Our investigation is also based on the information provided by the customer and our knowledge of the product.Results: visual inspection of the returned complaint opt970e optiflow + tracheostomy direct connection interface revealed that the tubing was found stretched and torn at the manifold.The complaint device was returned with the lanyard removed.Conclusion: we are unable to determine the cause of the reported damage to the subject opt970e optiflow + tracheostomy direct connection interface.However, based on our knowledge of the product and parts of the tubing being stretched, the reported event was likely caused by the cannula being subjected to excessive force.All optiflow interfaces are inspected during production for visual defects including cracks, tears, inclusions, discoloration and stretching or deformation.Any product that fails the visual inspection is disposed of.The subject opt970e optiflow + tracheostomy direct connection interface would have met the required specifications.The user instructions which accompany the opt970e optiflow + tracheostomy direct connection interface show in pictorial format the correct placement and fitting of the interface and states "to ensure loading and movement on tracheostomy tube is kept to a minimum, make sure the lanyard is secured properly." the user instructions also warn: "appropriate patient monitoring must be used at all times.Failure to monitor the patient may result in loss of therapy, serious injury or death." "do not crush or stretch tube, to prevent loss of therapy." "the lanyard is designed to minimize loading and movement of the tracheostomy tube.Secure the lanyard properly to avoid accidental decannulation or airway damage." "failure to use the set-up described above can compromise performance and affect patient safety.".

• Brand Name: OPTIFLOW + TRACHEOSTOMY INTERFACE
• Common Device Name: BTT
• Manufacturer (Section D): FISHER & PAYKEL HEALTHCARE LTD; 15 maurice paykel place; east tamaki; auckland, 2013 ; NZ 2013
• Manufacturer (Section G): FISHER & PAYKEL HEALTHCARE LTD; 15 maurice paykel place; east tamaki; auckland, 2013 ; NZ 2013
• Manufacturer Contact: faranak gomarooni ; 173 technology drive; suite 100; irvine, CA 92618 ; 9494534002
• MDR Report Key: 13256008
• Report Number: 9611451-2022-00037
• Device Sequence Number: 17324868
• Product Code: BTT
• UDI-Device Identifier: 09420012436924
• UDI-Public: (01)09420012436924(10)2101602439(11)210423
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K162553
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/20/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: OPT970E
• Device Catalogue Number: OPT970
• Device Lot Number: 2101602439
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/20/2021
• Supplement Date Received by Manufacturer: 03/20/2022
• Initial Report FDA Received Date: 01/13/2022
• Supplement Report FDA Received Date: 03/31/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/23/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: F&P PT100 MYAIRVO HUMIDIFIER; F&P PT101 AIRVO HUMIDIFIER
• Patient Sex: Unknown